Pevonedistat Granted FDA’s Breakthrough Therapy Status for Higher-Risk MDS: Takeda

August 3, 2020
Takeda Pharmaceutical said on July 30 that the US FDA has granted breakthrough therapy designation for its investigational drug pevonedistat for the treatment of patients with higher-risk myelodysplastic syndrome (HR-MDS). The drug is currently undergoing a PIII clinical study in...read more